共查询到20条相似文献,搜索用时 953 毫秒
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研究水溶盐结晶动力学需测定晶粒大小分布,作者使用新近发展起来的库尔特计数仪(Coulter Counter),结合电解质溶液的选择,成功地测定了氯化钾、氯化钠的晶粒。并对方法原理,非水悬浮剂选择,仪器定标及数据处理等进行如下讨论。一、原理使用英国产的TAⅡ型库尔特计数仪,又名16路多通道颗粒分析仪。测定方法是,先使待测物料均匀分散在电解质溶液中,借助负压,使微粒随溶液通过一小孔,孔两端各浸一铂电极,与检测系统构成闭合回路,其 相似文献
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介绍了Multisizer3库尔特粒子计数仪的原理、使用方法,并着重介绍了粘胶纤维生产过程中如何使用Multisizer3库尔特粒子计数仪检测粘胶中的颗粒。 相似文献
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0引言随着科技的发展,人们开发了多种基于不同工作原理的颗粒粒度的测量方法和测量仪器。最常见的有筛分法、沉降法、Coulter法和激光散射法等。筛分法只适用于粗粒度的测定,70μm以下的筛分就十分困难;Coulter法操作条件苛刻,只适于电解质中悬浮的粉体;激光散射法则有价格昂贵、调整困难、分辨率低和操作复杂等缺点。因而在工业上最常见的是沉降法〖1〗。上世纪80年代以来,我国相继开发了几种光透式沉降粒度分析仪,使我国沉降粒度分析水平得到了长足的发展。配合离心机的沉降粒度分析仪的测量范围通常在0.03~300μm,实际测量中设定的测量… 相似文献
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目的探讨显微镜与血细胞计数仪在血小板计数中的作用及其影响。方法对198例来院就诊体检人员进行血小板计数统计。结果正常标本计数无明显差异性(P>0.05),脂血标本和溶血标本计数比较,有明显的差异显著性(P<0.05)。结论显微镜与血细胞自动计数仪都是血小板计数的重要检测方法,在检测中重视2种方法影响和优势,对数据谨慎分析,确保检测结果的可信度和准确性,对临床治疗和用药提供有效的指导作用。 相似文献
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根据粘胶的溶解机理。在QB110C切割泵的作用下,通过考尔特ZB型粒子计数仪和电子显微镜(TEM)图片,分析了粘胶的粒子数和形态的变化。讨论了切割泵对粘胶溶解性及纺丝的影响。 相似文献
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Carefully sieved crystals of nickel ammonium sulphate are analysed with a Coulter particle size counter. Simple correction factors are proposed to rationalize the two sizing techniques. 相似文献
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D. B. Blackford 《Aerosol science and technology》2013,47(1):85-89
Large polystyrene spheres (nominally 5-, 7-, 10-, and 15-μm diameter) form a new range. The spheres have been sized using a Magiscan Image Analyzer, a scanning electron microscope, and a Coulter counter. Spheres of each nominal size have been found to have a tight size distribution. 相似文献
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R. K. Eckhoff 《应用聚合物科学杂志》1967,11(10):1855-1861
The volume frequency size distribution of PVC latex powder was determined by means of three different methods, which all gave the same frequency maximum at about 0.8–0.9 μ diameter. While the electron microscope analysis, which allows the agglomerates to be resolved into individual primary particles, did not show any particles above 1.5 μ in a sample of 9000, both the Coulter counter and the disk centrifuge showed a considerable amount of larger particles. 相似文献
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超细粉体粒度测试方法浅析 总被引:3,自引:0,他引:3
介绍了超细粉体粒度测试的几种主要方法(激光衍射散射法、离心沉降法、颗粒图像处理仪和库尔特颗粒计数器)的测试原理及性能特点,并进行了比较。讨论了粒度测试中应注意的几个问题,重点分析了测试条件不同对粒度测定的影响,得出分散介质、分散剂、超声功率及超声时间等是影响粒度测定的最主要的因素;指出了重复性、真实性、易操作性、量程和动态范围是评价粒度仪测试性能的几个重要指标。 相似文献
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The agglomeration of two TiO2 pigments (0.2-1.0μ) dispersed in an agitated 1% saline solution has been studied by a sequential count method using a Coulter counter. A model based on collision frequency due to the turbulent motion in a stirred vessel predicts the second order rate constant k to be proportional to agglomerate volume and to stirrer speed to the power 3/2. Experimental values of k were proportional to threshold volume to the power 0.79, stirrer speed to the power 1.3, and independent of TiO2 concentration 相似文献
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A simple light transmission instrument is described which enables average droplet sizes to be determined quickly and accurately. Light scattering is minimized by the use of a small-divergence laser beam and pinhole detectors, and by situating the sample photodetector relatively far from the sample. Good signal stability is ensured by the use of a double-beam configuration, the second beam serving as reference. The transmission of the sample is obtained from the time average ratio of the two signals. Use of a linearly polarized laser further increases accuracy and stability.Results of experiments with particles in the size range 0.8 – 50 μm show good agreement with Coulter counter analyses. 相似文献
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Kinetics of aggregation, nucleation and growth of canola protein particles were developed in a 100 mL mixed-suspension mixed-product removal precipitator (MSMPRP) using isoelectric precipitation with HCI at pH 4.2. Protein yield in terms of total nitrogen was measured by Kjeldahl system. The size distribution of protein aggregates was determined by a Coulter counter. The effects of pH, protein concentration driving force, mean residence time, agitation rate, ionic strength of the solution, and the operating temperature on the size distribution and yield of protein particles were investigated. Population balance on the protein particles was used to derive empirical correlations for the index of aggregation, nucleation rate of primary particles and growth rate of protein aggregates. 相似文献
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The porosity of poly (vinyl chloride) (PVC) resin particles produced in bulk polymerization is sensitive to polymerization conditions. Using scanning electron microscopy, 60μ spherical beads of PVC are shown to be composed of loosely packed 1μ spherical subparticles. This complex morphology is characterized by a variability in surface area. The surface area of bulk PVC materials can be measured by a chromatographic technique. The elution time of n-octane as a probe molecule on PVC packed columns is simply related to PVC surface area. At approximately constant particle size (measured by Coulter counter and optical microscopy), surface areas measured by argon adsorption are correlated to chromatographic elution times. The bulk density, plastisol viscosity and pore volume (from mercury penetration porosimetry) are determined and related to specific surface area. 相似文献
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D. P. Thibodeaux 《Journal of the American Oil Chemists' Society》1982,59(6):466A-472A
Analytical procedures have been developed for characterizing the size and shape of cotton dust particulates collected by the
vertical elutriator (VE) sampler. Data are reported for dust distributions on VE filters collected from different processing
areas (cleaning, delintering, hulling, and baling) in cottonseed oil mills. Results of particle volume distributions obtained
with a Coulter counter are compared with data obtained from an image-analysis system designed to classify cotton dust into
fibrous and nonfibrous (particulate) components. The image-analysis data include distributions of the lengths and widths of
fibers and the areas and diameters of particles present on the VE filters. In many of the locations studied, a considerable
amount of the total dust sampled can be attributed to lint, lint fragments, and also to particles significantly larger than
15 μm diameter.
Southern Region, SEA, USDA. 相似文献
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Highly porous particles furnish, due to their porosity, smaller Coulter diameters and Coulter volumes than the real particle size and envelope volume, respectively. Finding a relation between these variables (eqn. 4) makes the determination of the latter easier. In addition to the readily obtainable Coulter and porosity data, only one empirical constant for each material class has to be determined. 相似文献